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临床试验/NCT00426296
NCT00426296Unknown4 期

An Open-Label, Multicenter Study to Evaluate the Efficacy and Safety of a Fixed-Dose Combination of Abacavir 600 mg/Lamivudine 300 mg Once-Daily in Combination With Atazanavir 300 mg + Ritonavir 100 mg Once-Daily in Antiretroviral-Naïve HIV-1 Infected Subjects With Continuing Evaluation of Abacavir/Lamivudine Plus Atazanavir 400 mg for Maintenance Over an Additional 48 Weeks

Clinical Alliance for Research & Education - Infectious Diseases, LLC.2 个研究点 分布在 1 个国家开始时间: 2006年8月1日最近更新:
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相关药物

试验速览

阶段
4 期
发起方
试验地点
2

研究概览

简要总结

SHARE: Simple HAART with Abacavir, Reyataz, and Epivir

详细描述

Open-label, multicenter study of ABC/3TC + ATV in subjects who have completed at least 24 weeks of treatment on ABC/3TC+ATV/RTV as their first line regimen and have plasma HIV-1 RNA <50 copies/mL at entry

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Currently taking abacavir/lamivudine (Epzicom) in combination with atazanavir (Reyataz) boosted with ritonavir (Norvir) as first antiretroviral regimen
  • Viral load <50 copies/ml

排除标准

  • Viral load >50 copies/ml
  • Having taken more than one antiretroviral regimen

研究者

发起方
Clinical Alliance for Research & Education - Infectious Diseases, LLC.
申办方类型
Other

研究点 (2)

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